rs1800206, PPARA

N. diseases: 35
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Lipid Metabolism Disorders
CUI: C0154251
Disease: Lipid Metabolism Disorders
10 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2002 2002
Lipodystrophy
CUI: C0023787
Disease: Lipodystrophy
28 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1 2012 2012
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1 2008 2008
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2017 2017
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2009 2009
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2002 2002
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2013 2013
Nonalcoholic Steatohepatitis
CUI: C3241937
Disease: Nonalcoholic Steatohepatitis
17 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2005 2005
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2005 2005
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 0.010 1.000 1 2008 2008